EA001369B1 - Способ получения поликапролактама - Google Patents
Способ получения поликапролактама Download PDFInfo
- Publication number
- EA001369B1 EA001369B1 EA199900327A EA199900327A EA001369B1 EA 001369 B1 EA001369 B1 EA 001369B1 EA 199900327 A EA199900327 A EA 199900327A EA 199900327 A EA199900327 A EA 199900327A EA 001369 B1 EA001369 B1 EA 001369B1
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- polycaprolactam
- temperature
- carried out
- water
- pressure
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract description 12
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 title abstract description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 10
- 239000000203 mixture Substances 0.000 claims abstract description 7
- SCEIUGQQBYRBPP-UHFFFAOYSA-N 2,3,4,5-tetrahydro-1h-azepine Chemical compound C1CCC=CNC1 SCEIUGQQBYRBPP-UHFFFAOYSA-N 0.000 claims abstract description 6
- KBMSFJFLSXLIDJ-UHFFFAOYSA-N 6-aminohexanenitrile Chemical compound NCCCCCC#N KBMSFJFLSXLIDJ-UHFFFAOYSA-N 0.000 claims abstract description 6
- 238000010438 heat treatment Methods 0.000 claims abstract description 6
- 229920002292 Nylon 6 Polymers 0.000 claims description 12
- 238000004519 manufacturing process Methods 0.000 abstract description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 125000003277 amino group Chemical group 0.000 description 4
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- 239000004952 Polyamide Substances 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 229920002647 polyamide Polymers 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 2
- 150000001735 carboxylic acids Chemical class 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- -1 for example Substances 0.000 description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
- 150000003951 lactams Chemical class 0.000 description 2
- 239000012299 nitrogen atmosphere Substances 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- FGSUUFDRDVJCLT-UHFFFAOYSA-N 3-methylazepan-2-one Chemical compound CC1CCCCNC1=O FGSUUFDRDVJCLT-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- UWHCKJMYHZGTIT-UHFFFAOYSA-N Tetraethylene glycol, Natural products OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 description 1
- 238000001632 acidimetric titration Methods 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 235000019445 benzyl alcohol Nutrition 0.000 description 1
- 210000000988 bone and bone Anatomy 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D201/00—Preparation, separation, purification or stabilisation of unsubstituted lactams
- C07D201/02—Preparation of lactams
- C07D201/08—Preparation of lactams from carboxylic acids or derivatives thereof, e.g. hydroxy carboxylic acids, lactones or nitriles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D223/00—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom
- C07D223/02—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom not condensed with other rings
- C07D223/06—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom not condensed with other rings with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D223/12—Nitrogen atoms not forming part of a nitro radical
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Other In-Based Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Catalysts (AREA)
- Polyamides (AREA)
- Mounting Of Bearings Or Others (AREA)
- Audible-Bandwidth Dynamoelectric Transducers Other Than Pickups (AREA)
- Polyesters Or Polycarbonates (AREA)
- Saccharide Compounds (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19517823A DE19517823A1 (de) | 1995-05-18 | 1995-05-18 | Verfahren zur Herstellung von Caprolactam |
| PCT/EP1996/001892 WO1996036601A1 (de) | 1995-05-18 | 1996-05-07 | Verfahren zur herstellung von caprolactam |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EA199900327A1 EA199900327A1 (ru) | 2000-10-30 |
| EA001369B1 true EA001369B1 (ru) | 2001-02-26 |
Family
ID=7761969
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EA199900327A EA001369B1 (ru) | 1995-05-18 | 1996-05-07 | Способ получения поликапролактама |
| EA199700401A EA000465B1 (ru) | 1995-05-18 | 1996-05-07 | Способ получения капролактама |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EA199700401A EA000465B1 (ru) | 1995-05-18 | 1996-05-07 | Способ получения капролактама |
Country Status (27)
| Country | Link |
|---|---|
| US (1) | US6683177B1 (cs) |
| EP (1) | EP0815078B1 (cs) |
| JP (1) | JPH11505231A (cs) |
| KR (1) | KR100437858B1 (cs) |
| CN (2) | CN1076017C (cs) |
| AT (1) | ATE236121T1 (cs) |
| AU (1) | AU705339B2 (cs) |
| BG (1) | BG64093B1 (cs) |
| BR (1) | BR9608787A (cs) |
| CA (1) | CA2218130A1 (cs) |
| CZ (1) | CZ290780B6 (cs) |
| DE (2) | DE19517823A1 (cs) |
| DK (1) | DK0815078T3 (cs) |
| EA (2) | EA001369B1 (cs) |
| ES (1) | ES2194994T3 (cs) |
| HU (1) | HU220771B1 (cs) |
| MX (1) | MX9708677A (cs) |
| MY (1) | MY124474A (cs) |
| NO (1) | NO308598B1 (cs) |
| NZ (1) | NZ308486A (cs) |
| PL (1) | PL186249B1 (cs) |
| PT (1) | PT815078E (cs) |
| SG (1) | SG75895A1 (cs) |
| SK (1) | SK154797A3 (cs) |
| TR (2) | TR199801491T2 (cs) |
| TW (1) | TW340113B (cs) |
| WO (1) | WO1996036601A1 (cs) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2735471B1 (fr) † | 1995-06-16 | 1997-08-22 | Rhone Poulenc Chimie | Procede de preparation de lactames |
| DE19718706A1 (de) | 1997-05-02 | 1998-11-05 | Basf Ag | Verfahren zur Herstellung cyclischer Lactame |
| DE19738463C2 (de) | 1997-09-03 | 1999-09-23 | Basf Ag | Verfahren zur Herstellung von Caprolactam |
| US6858728B2 (en) * | 2003-06-17 | 2005-02-22 | Invista North America S.A.R.L. | Method for making caprolactam from impure ACN in which THA is not removed until after caprolactam is produced |
| US6716977B1 (en) * | 2003-06-17 | 2004-04-06 | E. I. Du Pont De Nemours And Company | Method for making caprolactam from impure ACN wherein ammonia and water are removed from crude caprolactam in a simple separation step and then THA is removed from the resulting caprolactam melt |
| US7208632B2 (en) * | 2004-09-10 | 2007-04-24 | Invista North America S.A R.L. | Separation of 6-aminocapronitrile and hexamethylenediamine from a mixture comprising hexamethylenediamine, 6-aminocapronitrile and tetrahydroazepine |
| CN114453029B (zh) * | 2022-02-09 | 2023-12-19 | 厦门大学 | 一种氧化物表面处理方法及其在己内酰胺制6-氨基己腈反应的应用 |
Family Cites Families (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE749649C (de) * | 1931-09-16 | 1944-11-29 | Aus mehreren Teilen zusammengesetzter elektrischer Isolierkoerper fuer Hochspannung | |
| US2208598A (en) | 1938-09-24 | 1940-07-23 | Du Pont | Aliphatic amino-nitriles and process of producing them |
| US2301964A (en) * | 1941-09-12 | 1942-11-17 | Du Pont | Method of preparing lactams |
| US2357484A (en) * | 1941-09-12 | 1944-09-05 | Du Pont | Process for producing compounds containing an n-substituted amide group |
| DE749469C (de) * | 1942-01-14 | 1944-12-04 | Verfahren zur Herstellung einer stickstoffhaltigen Verbindung | |
| DE848654C (de) | 1950-08-19 | 1952-09-08 | Basf Ag | Verfahren zur Herstellung von partiellen Hydrierungsprodukten des Adipinsaeuredinitrils |
| DE836938C (de) | 1950-08-26 | 1952-04-17 | Basf Ag | Verfahren zur Herstellung von Amionitrilen |
| NL7412695A (nl) * | 1974-09-26 | 1976-03-30 | Stamicarbon | De bereiding van een 2-amino-pyrrolinederivaat. |
| NL7412694A (nl) | 1974-09-26 | 1976-03-30 | Stamicarbon | Werkwijze voor de bereiding van een pyrrolidon- -2. |
| EP0150295A3 (en) | 1983-12-19 | 1988-03-30 | Allied Corporation | Selective production of n-substituted amides by use of cu(o)/metallic oxides catalyst compositions |
| US4628085A (en) * | 1985-09-03 | 1986-12-09 | Allied Corporation | Use of silica catalyst for selective production of lactams |
| US5192399A (en) | 1991-01-30 | 1993-03-09 | E. I. Du Pont De Nemours And Company | Purification of aminonitriles or diamines |
| US5133838A (en) | 1991-02-28 | 1992-07-28 | E. I. Du Pont De Nemours And Company | Purification of 6-aminocapronitrile |
| US5151543A (en) | 1991-05-31 | 1992-09-29 | E. I. Du Pont De Nemours And Company | Selective low pressure hydrogenation of a dinitrile to an aminonitrile |
| US5162567A (en) * | 1992-02-27 | 1992-11-10 | E. I. Du Pont De Nemours And Company | Purification of 6-aminocapronitrile |
| DE4339648A1 (de) | 1993-11-20 | 1995-05-24 | Basf Ag | Verfahren zur Herstellung von Caprolactam |
| FR2714379B1 (fr) * | 1993-12-23 | 1996-02-02 | Rhone Poulenc Chimie | Procédé de préparation de lactame. |
| DE4441962A1 (de) * | 1994-11-25 | 1996-05-30 | Basf Ag | Verfahren zur Herstellung von Caprolactam |
| DE19500041A1 (de) * | 1995-01-03 | 1996-07-04 | Basf Ag | Verfahren zur kontinuierlichen Reinigung von aus 6-Aminocapronitril hergestelltem Roh-Caprolactam |
| DE19628805A1 (de) * | 1996-07-17 | 1998-01-22 | Basf Ag | Verfahren zur Herstellung von Caprolactam aus 6-Aminocapronitril |
-
1995
- 1995-05-18 DE DE19517823A patent/DE19517823A1/de not_active Withdrawn
-
1996
- 1996-05-02 TW TW085105278A patent/TW340113B/zh active
- 1996-05-07 BR BR9608787A patent/BR9608787A/pt not_active Application Discontinuation
- 1996-05-07 CZ CZ19973577A patent/CZ290780B6/cs not_active IP Right Cessation
- 1996-05-07 EA EA199900327A patent/EA001369B1/ru not_active IP Right Cessation
- 1996-05-07 CN CN96193999A patent/CN1076017C/zh not_active Expired - Fee Related
- 1996-05-07 PL PL96323390A patent/PL186249B1/pl not_active IP Right Cessation
- 1996-05-07 DK DK96919688T patent/DK0815078T3/da active
- 1996-05-07 ES ES96919688T patent/ES2194994T3/es not_active Expired - Lifetime
- 1996-05-07 DE DE59610304T patent/DE59610304D1/de not_active Expired - Fee Related
- 1996-05-07 MX MX9708677A patent/MX9708677A/es not_active IP Right Cessation
- 1996-05-07 PT PT96919688T patent/PT815078E/pt unknown
- 1996-05-07 NZ NZ308486A patent/NZ308486A/xx unknown
- 1996-05-07 CA CA002218130A patent/CA2218130A1/en not_active Abandoned
- 1996-05-07 US US08/952,208 patent/US6683177B1/en not_active Expired - Fee Related
- 1996-05-07 KR KR1019970708203A patent/KR100437858B1/ko not_active Expired - Fee Related
- 1996-05-07 MY MYPI96001707A patent/MY124474A/en unknown
- 1996-05-07 WO PCT/EP1996/001892 patent/WO1996036601A1/de not_active Ceased
- 1996-05-07 SK SK1547-97A patent/SK154797A3/sk unknown
- 1996-05-07 TR TR1998/01491T patent/TR199801491T2/xx unknown
- 1996-05-07 AU AU58148/96A patent/AU705339B2/en not_active Ceased
- 1996-05-07 EA EA199700401A patent/EA000465B1/ru not_active IP Right Cessation
- 1996-05-07 TR TR97/01387T patent/TR199701387T1/xx unknown
- 1996-05-07 SG SG1998004735A patent/SG75895A1/en unknown
- 1996-05-07 AT AT96919688T patent/ATE236121T1/de not_active IP Right Cessation
- 1996-05-07 HU HU9802505A patent/HU220771B1/hu not_active IP Right Cessation
- 1996-05-07 JP JP8534517A patent/JPH11505231A/ja not_active Withdrawn
- 1996-05-07 EP EP96919688A patent/EP0815078B1/de not_active Expired - Lifetime
-
1997
- 1997-11-12 BG BG102038A patent/BG64093B1/bg unknown
- 1997-11-17 NO NO975270A patent/NO308598B1/no unknown
-
2001
- 2001-11-12 CN CN01138433A patent/CN1421474A/zh active Pending
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM4A | Lapse of a eurasian patent due to non-payment of renewal fees within the time limit in the following designated state(s) |
Designated state(s): AM AZ KZ KG TJ TM |
|
| MM4A | Lapse of a eurasian patent due to non-payment of renewal fees within the time limit in the following designated state(s) |
Designated state(s): BY MD RU |